Package 0115-1324-10

Brand: fenofibric acid

Generic: fenofibric acid
NDC Package

Package Facts

Identity

Package NDC 0115-1324-10
Digits Only 0115132410
Product NDC 0115-1324
Description

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1324-10)

Marketing

Marketing Status
Marketed Since 2024-06-01
Brand fenofibric acid
Generic fenofibric acid
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a1c48695-091f-4924-acf4-a420be16939d", "openfda": {"nui": ["N0000175596"], "upc": ["0301151325104"], "unii": ["BGF9MN2HU1"], "rxcui": ["828373", "828379"], "spl_set_id": ["e73404c5-e0ee-48e9-8b09-7a00d7e18e6c"], "pharm_class_epc": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1324-10)", "package_ndc": "0115-1324-10", "marketing_start_date": "20240601"}], "brand_name": "Fenofibric Acid", "product_id": "0115-1324_a1c48695-091f-4924-acf4-a420be16939d", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Peroxisome Proliferator Receptor alpha Agonist [EPC]"], "product_ndc": "0115-1324", "generic_name": "FENOFIBRIC ACID", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fenofibric Acid", "active_ingredients": [{"name": "FENOFIBRIC ACID", "strength": "45 mg/1"}], "application_number": "ANDA200264", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}